Hand Sanitizer

Manufacturer: Travel Retail Global Inc. | Bath Concept Cosmetics (Dongguan) Co., Ltd
Effective date: 2023-10-31
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:58:32

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Rub drime sized amount between hands until dry. Supervise children in the use of this product. In the case of eye contact, rinse eyes thoroughly with water.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Keep away from fire and flame Flammable,
Does not contain grain alcohol; do not drink. If taken internally serious gastric disturbances will result.

When using this product

OTC - WHEN USING SECTION

Avoid the eyes and mucous membrances
In the case of eyes or mucous membranes contact, rinse area thoroughly with water
In case of deep or puncture wounds or serious burns, consult physician.
If redness, irritation, swelling, or pain persists or increases or if infection occurs discontinue use and consult physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed,contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub drime sized amount between hands until dry.
Supervise children in the use of this product.
In the case of eye contact, rinse eyes thoroughly with water.

Other information

SPL UNCLASSIFIED SECTION

Store below 105 °F
May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe Barbadensis Leaf Juice, Carbomer, Triethanolamine.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	2
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	2
1305100	ethanol 75 % Topical Gel	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77129-001-50	Hand Sanitizer	50 mL in 1 BOTTLE	GEL	50		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77129-001	HAND SANITIZER (ALCOHOL) GEL [TRAVEL RETAIL GLOBAL INC.]	2	Current NDC, Legacy NDC, 1 package rows	20231101_62ec5bf1-9467-4c9b-b83d-6709f2146e0a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
ALOE VERA LEAF
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77129-001	77129-001-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hand Sanitizer	ALCOHOL	Travel Retail Global Inc.	62ec5bf1-9467-4c9b-b83d-6709f2146e0a	2023-10-31	Warnings	Exact identifier ndc (package): 77129-001-50 ndc (product): 77129-001 ndc11 (package): 77129000150 spl id: 0905a832-fda0-67bd-e063-6294a90a77cd spl set id: 62ec5bf1-9467-4c9b-b83d-6709f2146e0a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.